Canonical Allele Identifier: CA375685256

Gene: ABO

Linked Data

• gnomAD v4: 9-133255971-C-T
• MyVariant Identifiers: chr9:g.136131358C>T (hg19) ; chr9:g.133255971C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255971C>T , CM000671.2:g.133255971C>T	GRCh38
NC_000009.11:g.136131358C>T , CM000671.1:g.136131358C>T	GRCh37
NC_000009.10:g.135121179C>T	NCBI36
NG_006669.1:g.21697G>A
NG_006669.2:g.24245G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.789G>A
ENST00000647353.1:n.54-4819G>A
ENST00000679909.1:c.28+19191G>A	ENSP00000506089.1:n.28+19191G>A
ENST00000453660.3:n.771G>A
ENST00000538324.2:c.757G>A	ENSP00000483018.1:p.Ala253Thr
ENST00000611156.4:c.757G>A	ENSP00000483265.1:p.Ala253Thr
NM_020469.2:c.760G>A	NP_065202.2:p.Ala254Thr
NM_020469.3:c.760G>A	NP_065202.2:p.Ala254Thr